Duke University/16 June 2009
From 2009.igem.org
(Difference between revisions)
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- | + | [[Team:Duke | Return]] | |
- | + | ||
- | Measured concentration of DNA fragments 1 and 2 | + | ==June 16, 2009== |
+ | *E: PCR with Bioplastics #2 as template and Phusion mix (done by Maggie), Gels to check PCRs | ||
+ | |||
+ | <pre> | ||
+ | 2x Phusion mix 25 ul | ||
+ | forward primer 2.5 ul | ||
+ | reverse primer 2.5 ul | ||
+ | DNA template (plasmid) 1 ul | ||
+ | H2O 19 ul | ||
+ | 50 ul | ||
+ | </pre> | ||
+ | |||
+ | *R: No bands for fragments 3, Bands for fragment 4 | ||
+ | *C: Cut out bands of fragment 4, PCR again to obtain fragment 3 | ||
+ | |||
+ | |||
+ | *E: Measured concentration of DNA fragments 1 and 2 | ||
+ | *R: Concentrations okay | ||
+ | *C: Do assembly PCR once enough of fragments 3 and 4 obtained |
Latest revision as of 16:40, 21 October 2009
June 16, 2009
- E: PCR with Bioplastics #2 as template and Phusion mix (done by Maggie), Gels to check PCRs
2x Phusion mix 25 ul forward primer 2.5 ul reverse primer 2.5 ul DNA template (plasmid) 1 ul H2O 19 ul 50 ul
- R: No bands for fragments 3, Bands for fragment 4
- C: Cut out bands of fragment 4, PCR again to obtain fragment 3
- E: Measured concentration of DNA fragments 1 and 2
- R: Concentrations okay
- C: Do assembly PCR once enough of fragments 3 and 4 obtained